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1.
Several studies have provided evidence for the enrichment of trace elements in coastal waters, particularly for copper. These enrichments have been attributed to diffusion from continental shelf sediments and to an influx of river water. We attempted to resolve between these sources by undertaking an extensive suite of measurements of trace metals (Cu, Ni, Cd), 226Ra and 228Ra in the surface waters of the Gulf of Mexico, along with trace metal profiles at 6 stations (April 1981 and December 1982). These data establish that enrichments of copper, nickel and cadmium occur in the shallow waters of the Gulf of Mexico. On the Mississippi continental shelf, high trace element concentrations (Cu, Ni: ～ 9 nmol/kg; Cd: ～ 200 pmol/kg) in lower-salinity waters (26‰) are similar to those observed in the Mississippi plume at the same salinity. This evidence suggests a river water source. On the other hand, trace element enrichments are also observed in the northern Gulf (Cu: +0.4 nmol/kg; Ni: +0.5 nmol/kg; Cd: +20 pmol/kg) which coincide with an increase in 228Ra but are not accompanied by decreased salinity. The excess of evaporation over precipitation in this region makes it possible that this water could be evaporated estuarine water; therefore, hydrographic observations cannot distinguish readily between river and shelf sources. A regional flux balance shows that most of the excess copper in the surface waters of the Florida Current can be supplied by the river-borne dissolved copper flux. Within the uncertainties of such calculations, the continental shelf copper flux must be less than or equal to the river flux.  相似文献   

2.
Vertical profiles of Cd, Zn, Ni, and Cu have been determined at three stations in the North Pacific and in the surface waters on a transect from Hawaii to Monterey, California. The distributions found are oceanographically consistent and provide a needed confirmation and extension of several recent studies on the marine geochemistries of these metals. Cadmium concentrations average 1.4 pmol/kg in surface waters of the central North Pacific and show a strong correlation with the labile nutrients, phosphate and nitrate, increasing to values of 1.1 nmol/kg at depths corresponding to the phosphate maximum. Zinc is depleted in surface waters of the central gyre to an average value of 0.07 nmol/kg and increases to a deep maximum of 9 nmol/kg exhibiting a strong correlation with the nutrient silicate. Nickel concentrations average 2.1 nmol/kg in surface central gyre waters and increase to a deep maximum of 11 nmol/kg. Nickel is best correlated with a combination of phosphate and silicate. Copper averages less than 0.5 nmol/kg in surface waters of the central North Pacific and increases gradually to values of 5 nmol/kg in bottom waters. The Cu profiles show evidence of intermediate and deep water scavenging. The involvement of these metals in the internal biogeochemical cycles of the sea is responsible for their distributions which are predictable on the basis of oceanographic parameters.  相似文献   

3.
Manganese in the North Pacific   总被引：1，自引：0，他引：1  
A quantitative and precise method for determination of dissolved Mn at the nanomole(nmol)/kg level in seawater has been developed and used to study the distribution of Mn in the northeast Pacific. Mn concentrations in the surface mixed layer decrease from 1.0 to 0.6 nmol/kg between the central gyre and the western boundary of the California Current, then increase to values from 2 to 6 nmol/kg near the coastal boundary (in contrast to the distribution of210Pb). Particulate Mn in the surface waters accounts for only about 1% of the total.Vertical distributions of Mn are characterized by surface maxima, minima near 300 m, maxima at mid-depth coinciding with the oxygen minimum and the labile nutrient maxima, and concentrations in Pacific bottom waters of approximately 0.2 nmol/kg. The oceanic distribution of Mn appears to be dominated by external inputs superimposed upon overall scavenging which can lead to Mn maxima in (1) the surface waters due to riverine and atmospheric sources; (2) the deep ocean as a result of hydrothermal injection and/or sediment resuspension; and (3) the oxygen minimum region resulting from in-situ breakdown of organic matter, in-situ MnO2 reduction, and/or advective-diffusive transport of dissolved Mn from anoxic slope sediments.  相似文献   

4.
Two research cruises on the Baltic Sea, in July and November of 1979, were made for investigating the Baltic Sea water for its contents of dissolved cadmium, lead and copper. Atomic absorption spectrophotometry and voltammetry were used as methods of investigation, the latter method having supplied slightly lower results. In the water layer of 0 … 50 m the cadmium concentrations were 0.03 … 0.05 μg/l and the lead concentrations were 0.1 … 0.2 μg/l, seasonal changes did not have any effect on them. The copper concentrations, on the other hand, were 0.4 … 1.2 μg/l in summer and 0.1 … 0.7 μg/l in autumn. Compared with ocean waters, the lead content is remarkably high. In anoxic deep waters of the Baltic Sea the concentrations of the three metals, especially that of cadmium, are very low (< 0.01 μg/l).  相似文献   

5.
The toxic effect of copper on phytoplankton production is investigated in waters having different complexing capacities. It is demonstrated that a water’s complexing capacity does not guarantee that an equivalent amount of copper could be tolerated without adversely affecting algal production. Possible explanations for these findings are offered and discussed. It is deduced that ionic copper probably is already toxic to planktonic algae at concentrations of about 10?10 mole/l.  相似文献   

6.
We investigated the effect of acid mine drainage (AMD) from an abandoned copper mine at Britannia Beach (Howe Sound, BC, Canada) on primary productivity and chlorophyll a levels in the receiving waters of Howe Sound before, during, and after freshet from the Squamish River. Elevated concentrations of copper (integrated average through the water column >0.050 mg l−1) in nearshore waters indicated that under some conditions a small gyre near the mouth of Britannia Creek may have retained the AMD from Britannia Creek and from a 30-m deep water outfall close to shore. Regression and correlation analyses indicated that copper negatively affected primary productivity during April (pre-freshet) and November (post-freshet). Negative effects of copper on primary productivity were not supported statistically for July (freshet), possibly because of additional effects such as turbidity from the Squamish River. Depth-integrated average and surface chlorophyll a were correlated to copper concentrations in April. During this short study we demonstrated that copper concentrations from the AMD discharge can negatively affect both primary productivity and the standing stock of primary producers in Howe Sound.  相似文献   

7.
A survey of waters adjacent to this heavily urbanized and industrialized region showed concentrations of copper, 65 μg l.?1 to be the highest reported to date for estuarine waters, and lead up to 13.9 μg l.?1 Correlations between distributions of dissolved and total metal concentration in the water column, hydrography, and metal in the sediment were related to benthic studies in this area. Laboratory studies are cited which show the potential for adverse effects on marine animals at these metal concentrations.  相似文献   

8.
The general form of Cu-depth profiles is unique. In the central North Pacific, values decrease from a surface maximum of about 3 nmol/kg to 1.5 nmol/kg in the upper thermocline. Below about 750 m there is an increase to over 6 nmol/kg in the bottom waters with no mid-depth extremum. The profiles in the boundary regions are similar in the deep water but do not have the surface maximum. This unique elemental distribution is maintained by aeolean input to the surface waters comparable in magnitude to the fluvial component, ubiquitous scavenging in the subsurface and deep water, and a strong bottom source. Apparently the scavenging agent, presumably sinking particles, loses its Cu-binding capacity during early diagenesis. The half-life with respect to scavenging is about 1100 years and the overall residence time with respect to input or final removal about 5000 years.  相似文献   

9.
Anthropogenic mercury pollution was studied in Kastela Bay (Croatia), 10 years after chloralkaline plant (PVC) stopped production. The concentration of total mercury determined in sediments which are composed mainly of calcite and quartz, are in the range 14,280-30,400 ng/g. The values are higher than reported in the literature for Elbe and Seine estuaries and also above 25,000 ng/g used for criterion in remediation project in Minamata Bay. The concentration of methylmercury 6.05-36.74 ng/g are typical for slightly to highly contaminated estuarine sediments. The low ratio of methylmercury to total mercury found in sediments of Kastela Bay is in the range 0.04-0.18%. It can be explained that in this region predominate conditions which do not promote in-situ methylation. Sediments were found to be highly anoxic. Concentrations of total mercury in unfiltered surface waters are in the range 69-145 ng/l and in unfiltered bottom waters in the range 230-1,418 ngl(-1). High concentrations found in bottom waters suggest that either resuspension or partial dissolution of sediments takes place. An experiment performed on filtered and unfiltered waters showed that about 85% of total mercury in surface water and almost 100% in bottom water was retained on 45 microm filters. To demonstrate contrasts, two pristine estuaries from norths and south Europe were studied. Silicious sediments of Ore estuary (Sweden) and calcareous sediments of Krka estuary (Croatia) have total mercury concentrations close to accepted background level. The ratio of methylmercury to total mercury is < or = 1% in all samples with one exception. The highest observed ratio (2.70%) was in the surface sediment from E2 station in Krka estuary measured in March 2000. This location is suitable for studying methylmercury formation in pristine environment.  相似文献   

10.
The use of copper in antifouling paints has increased in the UK in the last 20 years as TBT and several other organic biocides have been phased out. To assess the probable impact of copper on estuarine systems a survey was undertaken to measure the different fractions of copper present in the water column at current usage. The different fractions measured were; labile copper, (LCu) considered as both the free copper ions and inorganically bound copper, the total dissolved copper (TDCu) present, and the difference between them taken as the organically bound likely non-toxic copper fraction. The survey considered sites with different levels of boat use, namely marinas, harbours and estuaries, differing physical parameters of suspended and dissolved organic matter, different seasons of the year and different depths in the water column all of which control speciation behaviour. Suspended particulate matter (SPM) values were measured at all sites and increased from West to East coast locations (5.7-34.4 mg/l). Dissolved organic matter (DOM) values ranged from 0.58 to 2.2mg/l C. The total dissolved copper concentrations ranged from 0.30 to 6.68 microg/l, with labile fraction ranging from 0.02 to 2.69 microg/l, and most labile copper concentrations below 1 microg/l. None of the yearly mean copper measurements exceeded the 76/464/EEC EQS of 5 microg/l. Of the 306 measurements, only one dissolved copper value in one season was above 5 microg/l. This ratio of labile to total copper was between 10 and 30%. The results from this survey suggest that if toxicity of copper is due to the labile fraction then using the total dissolved copper concentrations as an indicator of impact overestimate the risk by a factor of four times.  相似文献   

11.
The coastal water bodies that separate from White Sea water area due to Kandalaksha coast rise are examined. The hydrological and hydrochemical characteristics of these water bodies are found to notably differ from these in the bays and straits connected with them. Extreme values of water temperature and salinity were recorded. High concentrations of oxygen (>20 mg/l) were recorded in the near-surface water layers and high concentrations of hydrogen sulfide (>90 mg/l) in bottom waters. The species composition of phyto- and zooplankton was found to be poor. The characteristics of enzymatic destruction in subsurface waters of lakes are an order of magnitude greater than those in White Sea open areas.  相似文献   

12.
Low concentrations of herbicides (up to 70 ng l(-1)), chiefly diuron (up to 50 ng l(-1)) were detected in surface waters associated with inter-tidal seagrass meadows of Zostera muelleri in Hervey Bay, south-east Queensland, Australia. Diuron and atrazine (up to 1.1 ng g(-1) dry weight of sediment) were detected in the sediments of these seagrass meadows. Concentration of the herbicides diuron, simazine and atrazine increased in surface waters associated with seagrass meadows during moderate river flow events indicating herbicides were washed from the catchment to the marine environment. Maximum herbicide concentration (sum of eight herbicides) in the Mary River during a moderate river flow event was 4260 ng l(-1). No photosynthetic stress was detected in seagrass in this study during low river flow. However, with moderate river flow events, nearshore seagrasses are at risk of being exposed to concentrations of herbicides that are known to inhibit photosynthesis.  相似文献   

13.
Pore water has been extracted from Boom Clay by mechanical squeezing. Clay cores were obtained from various boreholes, all drilled at the SCK·CEN domain (Mol, Belgium).In contrast to pore water collected from piezometers, high sulphate concentrations are measured in the squeezed pore water. The lowest sulphate concentrations (<60 mg/l) were measured in pore waters squeezed immediately after drilling. Higher sulphate concentrations were often measured in the pore water when the clay cores were preserved for some time (generally <500 mg/l SO42−, but sometimes up to 20,000 mg/l SO42−). Nevertheless, a relation between preservation time and sulphate content could not be retrieved. However, major ion concentrations were obviously correlated with the sulphate content in the squeezed waters. The observed evolution in chemical composition were explained by water–rock interactions considering the pyrite oxidation and the subsequent ion exchange and mineral dissolution reactions.  相似文献   

14.
The chemical effects of chronic petroleum input into a shallow water marsh were examined by measuring hydrocarbon levels and dissolved organic carbon content of sediments associated with two active oil fields in south Louisiana. Annual levels of total organic carbon in the surface waters of the oil fields were higher by 1 mg C/l. in the salt marsh and 5 mg C/l. in the fresh marsh than the respective controlsites. Average dissolved organic carbon concentrations in the interstitial waters of cores taken within the oil field environments were 105% higher than the control in the salt marsh and 43% higher than the control in the fresh marsh. Significantly lower ratios of C17 to pristane occurred in both oil field sediments; however, average odd-even predominance values were not indicative of petroleum contaminated sediments. The results indicate that microbial processes are responsible for dissolution of petroleum into dissolved organic carbon and that dissolved organic carbon concentrations may be a more significant measure of chronic petroleum input than hydrocarbon distribution.  相似文献   

15.
Activities of the extracellular enzymes ß-D-glucosidase, phosphatase, and leucine aminopeptidase were investigated in unpolluted waters to test the suitability of fluorigenic model substrates for measuring enzyme activities in water samples expected to sustain low levels of activity. The waters tested were surface running waters, shallow groundwaters, and deep groundwaters from water extraction wells. Enzyme activity was detected in all the waters tested, although some of the hydrolytic rates were at the lower limit of current analytical capability. Rates varied between 1.1 and 291 nmol/(L·h) for ß-D-glucosidase, between 9.2 and 320 nmol/(L·h) for phosphatase, and between 5.8 and 1560 nmol/(L·h) for leucine aminopeptidase. The method thus proved to be suitable for measuring low levels of extracellular enzyme activity in natural waters, but in any case, it is necessary to adapt the technique to the type of water investigated.  相似文献   

16.
Sea catfish (Arius felis) were exposed to aqueous solutions of reagent grade cupric chloride in artificial seawater (30.0±2.0‰, 21–23°C) in four static bioassays. The 24, 48, 72 and 96 h LC50 were calculated and found to be 5.43, 4.17, 3.57 and 2.40 mg l.?1 copper, respectively. Experimental concentrations of copper producing subtle behavioral changes in this species correspond to less than 0.3% of the 72 h LC50. Based on this comparison with literature values, a new, maximum ‘safe’ concentration for copper in marine waters of 0.01 mg l.?1 is proposed.  相似文献   

17.
The thorium isotope content of ocean water   总被引：1，自引：0，他引：1  
232Th concentrations of surface and deep Pacific Ocean waters are 0.01–0.02 dpm/1000 kg (60 pgm/kg). The230Th activity is 0.03–0.13 dpm/1000 kg in surface waters and 0.3–2.7 dpm/1000 kg in deep waters. Chemical residence times based on in situ production from parent isotopes are about the same for230Th and228Th in surface waters (1–5 years) but are ten times greater for230Th in deep waters (10–100 years). Apparently there are additional sources of230Th into deep waters. At MANOP site S manganese nodule tops are enriched in Th isotopes by adsorption of Th from seawater and not by incorporation of Th-rich particulates.  相似文献   

18.
Lead concentrations were determined by isotope dilution mass spectrometry in 34 surface- and deep-water samples collected in the northeast Pacific between Hawaii and California and off the California coast using a deep-water sampler protected against fouling by contamination from the ship and hydrowire. Measured concentrations lie more than one order of magnitude below previously published open ocean values and they show that in most cases 90% or more of the total lead is in a dissolved form. Lead concentrations are about 10-fold higher in surface and thermocline waters than in deep waters; values drop as low as 1 ng/kg (5 pmol/kg) below 3500 m depth. Lead profiles thus appear different compared to those of most trace metals, which show enrichment in deep waters compared to surface concentrations. Lead concentrations in surface waters increase from 5 to 15 ng/kg (25 to 75 pmol/kg) along a transect starting from a location 200 km off the California coast and continuing towards the center of the North Pacific Gyre. This increase is congruent with that observed for210Pb concentrations in the same waters sampled at the same time.Lead is supplied to the open North Pacific largely from the atmosphere, at a rate of about 60 ng/cm2 yr, which exceeds the prehistoric oceanic output flux of authigenic lead recorded in pelagic sediments about tenfold. This excess originates from emissions from smelters and combustion of leaded gasoline, overwhelming natural lead inputs that entered the ocean during prehistoric time probably largely through rivers. Vertical lead concentration profiles below the surface mixed layer are probably not in steady state. There, concentrations must be increasing in response to the increase of anthropogenic inputs because the estimated lead residence times are more than 20 years in the thermocline and about 80 years in deep waters. Based on an estimated 10-fold input and concentration increase since the mid-eighteenth century in the surface mixed layer in the central northeast Pacific, it is calculated that the 10 ng/kg average concentration between 100 and 900 m is 2 to 5 times larger, and the 1.8 ng/kg average concentration between 900 and 5000 m depth is about 2 times larger than it was in the mid-eighteenth century. Profiles of lead concentrations in the North Atlantic are expected to be shifted generally to larger values by a factor of 2 to 3 compared to those in the North Pacific because of the effects of greater industrial lead contamination, while lead concentration profiles in the South Pacific are expected to be shifted generally to lower values compared to the North Pacific by about this same factor because of the effects of lesser industrial lead contamination.  相似文献   

19.
Cadmium, lead and copper have been determined in the dissolved and particulate phase for surface waters of the northern North Sea. Dissolved cadmium and copper show concentration gradients associated with salinity fronts which mark the boundary between coastal and ocean waters; lead does not. The particulate phase is shown to represent only a small fraction of the total metal concentration. Processes likely to be responsible for the observed distribution are discussed.  相似文献   

20.
The results of studying the elemental composition of surface continental waters in the European Russia from tundra to arid zone are discussed. The relative concentrations of elements in the solid residue of waters from various natural-climatic zones are evaluated, and the enrichment or dispersion of continental waters by these elements are analyzed as compared with their clarkes in the rocks that occur in the catchment areas. The coefficients of migration in water are evaluated, and the major elements with respect to which surface waters enrich under anthropogenic load are identified. The territorial distribution of higher concentrations of the most hazardous elements in waters of lakes is characterized.  相似文献   

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